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Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience.
Saudi Med J. 2019 Jul;40(7):669-674. doi: 10.15537/smj.2019.7.24291.
Saudi Med J. 2019.
PMID: 31287126
Free PMC article.
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion.
Sansbury FH, Flanagan SE, Houghton JA, Shuixian Shen FL, Al-Senani AM, Habeb AM, Abdullah M, Kariminejad A, Ellard S, Hattersley AT.
Sansbury FH, et al. Among authors: al senani am.
Diabetologia. 2012 Sep;55(9):2381-5. doi: 10.1007/s00125-012-2595-0. Epub 2012 Jun 2.
Diabetologia. 2012.
PMID: 22660720
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